## Abstract Collisional activation spectra show that the [C~9~H~11~O] ion formed by loss of CH~2~OH from the title compound has rearranged to the protonated phenylacetone structure.
Collisional activation spectra. Behavior of [C3H7O]+ and other [CnH2n+1O]+ ions
β Scribed by F. W. McLafferty; Ikuo Sakai
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 698 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1076-5174
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β¦ Synopsis
Abstract
Collisional activation spectra have identified (i) as Stable ion structures. Evidence is presented for a variety of pathway for their formation, including anchimeric assistance and hydrogen migration in less stable isomers. The fragmentation behavior of a number of [C~n~H~2__n__+1~O]^+^ isomers of n = 2 to 5 shows that extensive rearrangements are common, but that some reactions appear to be useful for ion structure elucidation. One reaction identified is unusual in that it represents the decomposition of an evenβelectron ion to yied an oddβelectron ion product in significant abundance.
π SIMILAR VOLUMES
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The rate constants of the reactions of ethoxy (C 2 H 5 O), i-propoxy (i-C 3 H 7 O) and npropoxy (n-C 3 H 7 O) radicals with O 2 and NO have been measured as a function of temperature. Radicals have been generated by laser photolysis from the appropriate alkyl nitrite and have been detected by laser-
The unimolecular decompositions of two isomers of [C&N]+, CH3CH2CH=NH2 and CH3CHzh=CH,, are dis-ed in terms of the potential energy profile over which reaction may be considered to occur. The energy needed to promote slow (metastable) dissociations of either ion is found to be less than that require